Description
An atypical antipsychotic; binds to dopamine D1-4, α-adrenergic, and histamine receptors (Kis = 0.42-1.45, 0.32-1.26, and 1-6.17 nM, respectively), as well as various 5-HT receptors (Kis = 0.03-3.98 nM); inhibits DOI, apomorphine, or clonidine-induced neuron firing in rat brain (ED50s = 75, 40, and 85 μg/kg, respectively); increases mPFC, NAc, and lateral striatum extracellular dopamine and suppresses the conditioned avoidance response in rats from 0.05-0.2 mg/kg, s.c.; prevents acute and chronic phencyclidine-induced deficits in cued reversal learning in rats at 0.075 mg/kg
Formal name: rel-5-chloro-2,3,3aR,12bR-tetrahydro-2-methyl-1H-dibenz[2,3:6,7]oxepino[4,5-c]pyrrole
Synonyms:
Molecular weight: 285.8
CAS: 65576-45-6
Purity: ≥95%
Formulation: A solid